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[Rinsho ketsueki] The Japanese journal of clinical hematology · 2022

[Malignant paraganglioma mimicking multiple myeloma].

Клинический случайАннотация на английскомСтатьяНазвание и аннотация: Перевод в очереди
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Nagao Toshikage, Bando Kana, Iura Ayuko, Kakuta Ryota, Kano Yoshihito, Ikeda Sadakatsu, Nogami Ayako, Tanaka Yosuke, Kirimura Susumu, Mori Takehiko

Аннотация

We here present a 33-year-old woman who was referred to our hospital with a complaint of back pain and was found to have elevated IgG and hypercalcemia, as well as osteolytic lesions of pelvis and spines. 18F-FDG-PET/CT scan revealed numerous uptakes in the bones. An examination of the bone marrow revealed increased plasma cells (10.2%). Despite clinical similarities to multiple myeloma, any evidence of plasma cell clonal proliferation, including serum M-protein and light chain restriction, was not found. A reexamination of the bone marrow with a biopsy revealed the proliferation of abnormal cells with chromogranin A and synaptophysin expression but no expression of hematopoietic and epithelial cell markers. Based on these results together with extra-adrenal lesions, a diagnosis of malignant paraganglioma was made. Malignant paraganglioma is known to frequently cause bone metastasis and skeletal related events, whose clinical manifestations are similar to those of multiple myeloma. Since patients with osteolytic lesions, hypercalcemia, and hypergammaglobulinemia are likely to be referred to hematologists, malignant paraganglioma should be considered as a differential diagnosis.

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